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Results: 1-10 |
Results: 10
DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE-1A NEUROPATHY
Authors: ROA BB GREENBERG F GUNARATNE P SAUER CM LUBINSKY MS KOZMA C MECK JM MAGENIS RE SHAFFER LG LUPSKI JR
Citation: Bb. Roa et al., DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE-1A NEUROPATHY, Human genetics, 97(5), 1996, pp. 642-649
PRENATAL-DIAGNOSIS OF AN INFANT WITH MOSAIC TRISOMY-16 OF PATERNAL ORIGIN
Authors: PAULYSON KJ SHERER DM CHRISTIAN SL LEWIS KM LEDBETTER DH SALAFIA CM MECK JM
Citation: Kj. Paulyson et al., PRENATAL-DIAGNOSIS OF AN INFANT WITH MOSAIC TRISOMY-16 OF PATERNAL ORIGIN, Prenatal diagnosis, 16(11), 1996, pp. 1021-1026
ADENOMYOSIS - EVIDENCE FOR GENETIC CAUSE
Authors: ARNOLD LL MECK JM SIMON JA
Citation: Ll. Arnold et al., ADENOMYOSIS - EVIDENCE FOR GENETIC CAUSE, American journal of medical genetics, 55(4), 1995, pp. 505-506
DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE 1A NEUROPATHY
Authors: ROA BB GREENBERG F GUNARATNE P SAUER CM LUBINSKY MS KOZMA C MECK JM MAGENIS RE SHAFFER LG LUPSKI JR
Citation: Bb. Roa et al., DUPLICATION OF THE PMP22 GENE IN 17P PARTIAL TRISOMY PATIENTS WITH CHARCOT-MARIE-TOOTH TYPE 1A NEUROPATHY, American journal of human genetics, 57(4), 1995, pp. 171-171
AN UNUSUAL CASE OF TRISOMY-16 MOSAICISM DUE TO PATERNAL NONDISJUNCTION
Authors: MECK JM CHRISTIAN SL PAULYSON KJ SIQUES MJ LEWIS K GARNICA A SEYDEL FD LEDBETTER DH
Citation: Jm. Meck et al., AN UNUSUAL CASE OF TRISOMY-16 MOSAICISM DUE TO PATERNAL NONDISJUNCTION, American journal of human genetics, 57(4), 1995, pp. 674-674
KERATINOCYTES IMMORTALIZED BY HUMAN PAPILLOMAVIRUS-18 EXHIBIT ALTERATIONS DEPENDENT UPON HOST GENETIC BACKGROUND AND COMPLEXITY OF VIRAL GENES TRANSFECTED
Authors: PEI XF QIN NG MECK JM SCHLEGEL R
Citation: Xf. Pei et al., KERATINOCYTES IMMORTALIZED BY HUMAN PAPILLOMAVIRUS-18 EXHIBIT ALTERATIONS DEPENDENT UPON HOST GENETIC BACKGROUND AND COMPLEXITY OF VIRAL GENES TRANSFECTED, Pathobiology, 62(1), 1994, pp. 43-52
PRENATAL-DIAGNOSIS OF TRISOMY-12 MOSAICISM - PHYSICAL AND DEVELOPMENTAL FOLLOW-UP
Authors: MECK JM KOZMA C TCHABO JG KING JC LENCKI S PINCKERT TL
Citation: Jm. Meck et al., PRENATAL-DIAGNOSIS OF TRISOMY-12 MOSAICISM - PHYSICAL AND DEVELOPMENTAL FOLLOW-UP, Prenatal diagnosis, 14(9), 1994, pp. 878-883
FAMILIAL 10P TRISOMY RESULTING FROM A MATERNAL PERICENTRIC-INVERSION
Authors: KOZMA C MECK JM
Citation: C. Kozma et Jm. Meck, FAMILIAL 10P TRISOMY RESULTING FROM A MATERNAL PERICENTRIC-INVERSION, American journal of medical genetics, 49(3), 1994, pp. 281-287
COTRANSFECTION OF HPV-18 AND V-FOS DNA INDUCES TUMORIGENICITY OF PRIMARY HUMAN KERATINOCYTES
Authors: PEI XF MECK JM GREENHALGH D SCHLEGEL R
Citation: Xf. Pei et al., COTRANSFECTION OF HPV-18 AND V-FOS DNA INDUCES TUMORIGENICITY OF PRIMARY HUMAN KERATINOCYTES, Virology, 196(2), 1993, pp. 855-860
2 CASES OF MOSAIC VARIEGATED ANEUPLOIDY WITH MICROCEPHALY - A MUTATION THAT RESULTS IN MITOTIC NONDISJUNCTION
Authors: STETKA DG BICK DP MECK JM BATY EB SCHULMAN JD
Citation: Dg. Stetka et al., 2 CASES OF MOSAIC VARIEGATED ANEUPLOIDY WITH MICROCEPHALY - A MUTATION THAT RESULTS IN MITOTIC NONDISJUNCTION, American journal of human genetics, 53(3), 1993, pp. 604-604
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